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        <datestamp>2026-09-14T15:27:09Z</datestamp>
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          <dc:title>OxLDL_Mdivi_qPCR.csv</dc:title>
          <dc:creator>Brandt Pence (4630597)</dc:creator>
          <dc:subject>Cellular immunology</dc:subject>
          <dc:subject>Geriatrics and gerontology</dc:subject>
          <dc:subject>Cardiology (incl. cardiovascular diseases)</dc:subject>
          <dc:subject>inflammaging</dc:subject>
          <dc:subject>OxLDL</dc:subject>
          <dc:subject>atherosclerosis</dc:subject>
          <dc:subject>monocytes</dc:subject>
          <dc:description>&lt;p dir="ltr"&gt; and  contain qPCR data from gene expression experiments. Cells from Seahorse assays were lysed in Trizol and processed for mRNA isolation and reverse transcription to cDNA. Both datasets are similarly structured.&lt;/p&gt;&lt;p dir="ltr"&gt;Column 1 [Sample] is an internal number used for sample storage and location.&lt;/p&gt;&lt;p dir="ltr"&gt;Column 2 [Subj] is a recoded subject number used for pairing in statistical tests.&lt;/p&gt;&lt;p dir="ltr"&gt;Column 3 [Plate] is a plate number.&lt;/p&gt;&lt;p dir="ltr"&gt;Column 4 [Treat] is treatment condition. [Med = media only; OxLDL = OxLDL only; MDIVI = OxLDL + Mdivi-1; S1QEL = OxLDL + S1QEL]&lt;/p&gt;&lt;p dir="ltr"&gt;Columns 5-8 are relative gene expression values calculated using the ddCt method for the genes IL1B, IL6, CXCL8, and TNF respectively.&lt;/p&gt;&lt;p&gt;&lt;br&gt;&lt;/p&gt;</dc:description>
          <dc:date>2026-09-14T15:27:09Z</dc:date>
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